Hydrochloric Acid → HCID 10133649, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[S:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)=[CH:8][CH:7]=1.[CH2:21]([NH:24][CH2:25][CH2:26][CH3:27])[CH2:22][CH3:23].Cl>>[CH2:21]([N:24]([CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[S:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)=[CH:8][CH:7]=1)[CH2:25][CH2:26][CH3:27])[CH2:22][CH3:23]Participants
4
Procedure
The title compound was prepared as described in Example 43 starting with (I) of Example 43 (2.0 g, 6.3 mmol) and using dipropylamine in place of dibutylamine to produce 0.41 g (19% yield) of the title compound as the HCl salt, mp 142°-143° C. IR(KBr): 3400, 1600 cm-1. MS: 369(MH+). 1H NMR (CDCl3): δ 8.19-6.95 (m, 8H), 4.19 (t, J=5.1 Hz, 2H), 3.01 (m, 6H), 2.64-0.82 (m, 12H).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-02dffdd7c06e4f6e9e30eccb72326465
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04861897
Reaction notes
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